Canonical Allele Identifier: CA471816696
Gene: MGMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.131565253C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766989C>A , CM000672.2:g.129766989C>A GRCh38
NC_000010.10:g.131565253C>A , CM000672.1:g.131565253C>A GRCh37
NC_000010.9:g.131455243C>A NCBI36
NG_052673.1:g.304806C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.709C>A ENSP00000302111.7:p.Arg237=
ENST00000651593.1:c.616C>A MANE Select ENSP00000498729.1:p.Arg206=
ENST00000306010.7:c.709C>A ENSP00000302111.7:p.Arg237=
NM_002412.3:c.709C>A NP_002403.2:p.Arg237=
NM_002412.4:c.709C>A NP_002403.2:p.Arg237=
XM_005252682.2:c.616C>A XP_005252739.1:p.Arg206=
XM_006717863.2:c.439C>A XP_006717926.1:p.Arg147=
XM_011539817.1:c.625C>A XP_011538119.1:p.Arg209=
NM_002412.5:c.616C>A MANE Select NP_002403.3:p.Arg206=
XM_017016275.1:c.439C>A XP_016871764.1:p.Arg147=